Ring opening polymerization of macrolactones: high conversions and activities using an yttrium catalyst

dc.contributor.authorMyers, D.
dc.contributor.authorWitt, Timo
dc.contributor.authorCyriac, A.
dc.contributor.authorBown, Mark
dc.contributor.authorMecking, Stefan
dc.contributor.authorWilliams, Charlotte K.
dc.date.accessioned2017-12-13T08:16:55Z
dc.date.available2017-12-13T08:16:55Z
dc.date.issued2017eng
dc.description.abstractThe ring-opening polymerization of macrolactones (C15–C23) enables the production of long-chain aliphatic polyesters which are crystalline polymers with melting temperatures ranging from 98–106 °C. Here, the polymerization of ω-pentadecalactone (C15), nonadecalactone (C19) and tricosalactone (C23) are investigated using an yttrium phosphasalen catalyst. The catalyst enables typical conversions to exceed >80% and the reactions occur either in neat monomer or in solution in toluene, over the temperature range 25–100 °C. The yttrium catalyst shows higher activities than previously reported aluminium–salen complexes, with TOF values in the range 200–400 h−1 in the best cases. The polymerizations occur with linear increase in molecular weight vs. conversion and enable the production of polyester with 10 < Mn< 60 kg mol−1. Using tricosalactone the polymerization thermodynamic parameters are determined and confirm the polymerization is entropically driven. The findings underscore the importance of continued catalyst development to allow higher rates of reaction which has the added benefit of accessing the highest conversions to polymer.eng
dc.description.versionpublishedde
dc.identifier.doi10.1039/c7py00985beng
dc.identifier.ppn496359274
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/40903
dc.language.isoengeng
dc.rightsterms-of-use
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dc.subject.ddc540eng
dc.titleRing opening polymerization of macrolactones: high conversions and activities using an yttrium catalysteng
dc.typeJOURNAL_ARTICLEde
dspace.entity.typePublication
kops.citation.bibtex
@article{Myers2017openi-40903,
  year={2017},
  doi={10.1039/c7py00985b},
  title={Ring opening polymerization of macrolactones: high conversions and activities using an yttrium catalyst},
  number={37},
  volume={8},
  issn={1759-9954},
  journal={Polymer Chemistry},
  pages={5780--5785},
  author={Myers, D. and Witt, Timo and Cyriac, A. and Bown, Mark and Mecking, Stefan and Williams, Charlotte K.}
}
kops.citation.iso690MYERS, D., Timo WITT, A. CYRIAC, Mark BOWN, Stefan MECKING, Charlotte K. WILLIAMS, 2017. Ring opening polymerization of macrolactones: high conversions and activities using an yttrium catalyst. In: Polymer Chemistry. 2017, 8(37), pp. 5780-5785. ISSN 1759-9954. eISSN 1759-9962. Available under: doi: 10.1039/c7py00985bdeu
kops.citation.iso690MYERS, D., Timo WITT, A. CYRIAC, Mark BOWN, Stefan MECKING, Charlotte K. WILLIAMS, 2017. Ring opening polymerization of macrolactones: high conversions and activities using an yttrium catalyst. In: Polymer Chemistry. 2017, 8(37), pp. 5780-5785. ISSN 1759-9954. eISSN 1759-9962. Available under: doi: 10.1039/c7py00985beng
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    <dcterms:abstract xml:lang="eng">The ring-opening polymerization of macrolactones (C15–C23) enables the production of long-chain aliphatic polyesters which are crystalline polymers with melting temperatures ranging from 98–106 °C. Here, the polymerization of ω-pentadecalactone (C15), nonadecalactone (C19) and tricosalactone (C23) are investigated using an yttrium phosphasalen catalyst. The catalyst enables typical conversions to exceed &gt;80% and the reactions occur either in neat monomer or in solution in toluene, over the temperature range 25–100 °C. The yttrium catalyst shows higher activities than previously reported aluminium–salen complexes, with TOF values in the range 200–400 h−1 in the best cases. The polymerizations occur with linear increase in molecular weight vs. conversion and enable the production of polyester with 10 &lt; Mn&lt; 60 kg mol−1. Using tricosalactone the polymerization thermodynamic parameters are determined and confirm the polymerization is entropically driven. The findings underscore the importance of continued catalyst development to allow higher rates of reaction which has the added benefit of accessing the highest conversions to polymer.</dcterms:abstract>
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kops.sourcefieldPolymer Chemistry. 2017, <b>8</b>(37), pp. 5780-5785. ISSN 1759-9954. eISSN 1759-9962. Available under: doi: 10.1039/c7py00985bdeu
kops.sourcefield.plainPolymer Chemistry. 2017, 8(37), pp. 5780-5785. ISSN 1759-9954. eISSN 1759-9962. Available under: doi: 10.1039/c7py00985bdeu
kops.sourcefield.plainPolymer Chemistry. 2017, 8(37), pp. 5780-5785. ISSN 1759-9954. eISSN 1759-9962. Available under: doi: 10.1039/c7py00985beng
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source.periodicalTitlePolymer Chemistryeng

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